A citation-based method for searching scientific literature


List of co-cited articles
269 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
139
32

Research with stored biological samples: what do research participants want?
Donna T Chen, Donald L Rosenstein, Palaniappan Muthappan, Susan G Hilsenbeck, Franklin G Miller, Ezekiel J Emanuel, David Wendler. Arch Intern Med 2005
81
28

High rate of consent to bank biologic samples for future research: the Eastern Cooperative Oncology Group experience.
Thomas Malone, Paul J Catalano, Peter J O'Dwyer, Bruce Giantonio. J Natl Cancer Inst 2002
57
35




Public attitudes regarding the donation and storage of blood specimens for genetic research.
S S Wang, F Fridinger, K M Sheedy, M J Khoury. Community Genet 2001
98
20

Consent to the use of stored DNA for genetics research: a survey of attitudes in the Jewish population.
M D Schwartz, K Rothenberg, L Joseph, J Benkendorf, C Lerman. Am J Med Genet 2001
47
31


Consent for genetic research in a general population: the NHANES experience.
Geraldine M McQuillan, Kathryn S Porter, Maria Agelli, Raynard Kington. Genet Med 2003
125
18

The ethics of research using biobanks: reason to question the importance attributed to informed consent.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Arch Intern Med 2005
71
18

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
232
16

Informed consent for population-based research involving genetics.
L M Beskow, W Burke, J F Merz, P A Barr, S Terry, V B Penchaszadeh, L O Gostin, M Gwinn, M J Khoury. JAMA 2001
185
14



Research on stored biological samples: views of African American and White American cancer patients.
Rebecca D Pentz, Laurent Billot, David Wendler. Am J Med Genet A 2006
65
16



Obtaining 'fresh' consent for genetic research with biological samples archived 10 years ago.
Eric Vermeulen, Marjanka K Schmidt, Neil K Aaronson, Marianne Kuenen, Flora E van Leeuwen. Eur J Cancer 2009
27
33

Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns.
Aaro Tupasela, Sinikka Sihvo, Karolna Snell, Pa Jallinoja, Arja R Aro, Elina Hemminki. Scand J Public Health 2010
50
18

Informed consent for genetic research on stored tissue samples.
E W Clayton, K K Steinberg, M J Khoury, E Thomson, L Andrews, M J Kahn, L M Kopelman, J O Weiss. JAMA 1995
202
10

Patients' views on residual blood use for research purposes.
N Hamajima, K Tajima, H Oya, T Kato, K Okuma, H Kaneda, S Moritaka, T Kato. Jpn J Cancer Res 1998
10
80

Ownership and uses of human tissue: does the Nuffield bioethics report accord with opinion of surgical inpatients?
R D Start, W Brown, R J Bryant, M W Reed, S S Cross, G Kent, J C Underwood. BMJ 1996
25
32

Willingness to donate blood samples for genetic research: a survey from a community in Singapore.
M L Wong, K S Chia, W M Yam, G R Teodoro, K W Lau. Clin Genet 2004
56
14


Trends in ethical and legal frameworks for the use of human biobanks.
A Cambon-Thomsen, E Rial-Sebbag, B M Knoppers. Eur Respir J 2007
157
10



Cancer patients' attitudes toward future research uses of stored human biological materials.
Paul R Helft, Victoria L Champion, Rachael Eckles, Cynthia S Johnson, Eric M Meslin. J Empir Res Hum Res Ethics 2007
40
20

DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
70
10



The ethical use of existing samples for genome research.
Oliver F Bathe, Amy L McGuire. Genet Med 2009
33
21



Bio-libraries and DNA storage: assessment of patient perception of information.
G Moutel, S de Montgolfier, J P Meningaud, C Hervé. Med Law 2001
14
42

Human genetic research, DNA banking and consent: a question of 'form'?
M Deschênes, G Cardinal, B M Knoppers, K C Glass. Clin Genet 2001
57
10


Attitudes and perceptions of patients towards methods of establishing a DNA biobank.
Jill M Pulley, Margaret M Brace, Gordon R Bernard, Dan R Masys. Cell Tissue Bank 2008
75
8

Patients' views on identifiability of samples and informed consent for genetic research.
Sara Chandros Hull, Richard R Sharp, Jeffrey R Botkin, Mark Brown, Mark Hughes, Jeremy Sugarman, Debra Schwinn, Pamela Sankar, Dragana Bolcic-Jankovic, Brian R Clarridge,[...]. Am J Bioeth 2008
81
8

Research ethics recommendations for whole-genome research: consensus statement.
Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh,[...]. PLoS Biol 2008
156
8

Attitudes of the Japanese public and doctors towards use of archived information and samples without informed consent: preliminary findings based on focus group interviews.
Atsushi Asai, Motoki Ohnishi, Etsuyo Nishigaki, Miho Sekimoto, Shunichi Fukuhara, Tsuguya Fukui. BMC Med Ethics 2002
24
20

Awareness and motivation of Japanese donors of blood for research.
T Nakayama, K Muto, N Yoshiike, T Yokoyama. Am J Public Health 1999
10
50

Navigating an ethical patchwork--human gene banks.
Karen J Maschke. Nat Biotechnol 2005
35
14





Consent to using human tissue.
Peter Furness. BMJ 2003
19
26


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.